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.glm.linear

Linear regression from --glm (quantitative phenotype). Header line starts with '#'. Column set can be reduced with cols=; optional NEG_LOG10_P and joint F_STAT appear with modifiers.

Overview

Field Value
Format key plink2_linear
Spec file formats/plink2_linear.json
Cite name PLINK 2.0
Version PLINK 2.0 (doc revision 11 Mar 2026)
Last checked 20260326
Source https://www.cog-genomics.org/plink/2.0/formats#glm_linear
Citation Chang, C. C., Chow, C. C., Tellier, L. C., Vattikuti, S., Purcell, S. M., & Lee, J. J. (2015). Second-generation PLINK: rising to the challenge of larger and richer datasets. Gigascience, 4(1), s13742-015.
## File layout
Field Value
Separator TAB
NA value .
Comment prefix #
Header row yes
Column order #CHROM, POS, ID, REF, ALT1, ALT, PROVISIONAL_REF?, A1, OMITTED, A1_CT, ALLELE_CT, A1_FREQ, MACH_R2, TEST, OBS_CT, BETA, SE, L95, U95, T_STAT, F_STAT, P, ERRCODE, LOG10_P
## Column mapping
Raw header Canonical Canonical (secondary)
#CHROM CHR
A1 EA
A1_CT
A1_FREQ EAF
ALLELE_CT
ALT ALT
ALT1
BETA BETA
CHROM CHR
ERRCODE
F_STAT F
ID SNPID rsID
L95 BETA_95L
LOG10_P MLOG10P
MACH_R2 INFO
OBS_CT N
OMITTED
P P
POS POS
PROVISIONAL_REF?
REF REF
SE SE
T_STAT T
TEST
U95 BETA_95U
## Header descriptions
Column Description
#CHROM Chromosome code
A1 Counted allele in regression
A1_CT Total A1 allele count
A1_FREQ A1 allele frequency
ALLELE_CT Allele observation count
ALT All alternate alleles (comma-separated)
ALT1 First alternate allele
BETA Regression coefficient for A1
ERRCODE Reason for NA result
F_STAT F-statistic (joint tests)
ID Variant ID
L95 Lower symmetric approx. CI for beta (--ci)
LOG10_P Optional -log10(p) column
MACH_R2 MaCH imputation R-squared
OBS_CT Samples in regression
OMITTED Omitted allele
P Asymptotic p-value
POS Base-pair coordinate
PROVISIONAL_REF? Whether REF is provisional
REF Reference allele
SE Standard error of beta
T_STAT t-statistic (linear model)
TEST Test identifier
U95 Upper symmetric approx. CI for beta (--ci)
## Coverage

8/9 tier groups satisfied.

Tier Status Matched Missing
Variant ID yes SNPID, rsID
Genomic location yes CHR, POS
Effect / other allele partial EA NEA
Effect size yes BETA OR, HR, Z
Uncertainty yes SE
P-value yes P, MLOG10P
Sample size yes N N_CASE
Allele frequency yes EAF MAF, NEAF
Imputation / QC yes INFO
## See also